ID: ALA4101808

Max Phase: Preclinical

Molecular Formula: C15H14N4O3

Molecular Weight: 298.30

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cc(C=O)c(OCc2cccn3c(C)nnc23)cn1

Standard InChI:  InChI=1S/C15H14N4O3/c1-10-17-18-15-11(4-3-5-19(10)15)9-22-13-7-16-14(21-2)6-12(13)8-20/h3-8H,9H2,1-2H3

Standard InChI Key:  ANDRSMSEUBWDCW-UHFFFAOYSA-N

Associated Targets(Human)

Hemoglobin HbA 880 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 298.30Molecular Weight (Monoisotopic): 298.1066AlogP: 1.83#Rotatable Bonds: 5
Polar Surface Area: 78.61Molecular Species: NEUTRALHBA: 7HBD: 0
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 2.63CX LogP: 0.42CX LogD: 0.42
Aromatic Rings: 3Heavy Atoms: 22QED Weighted: 0.67Np Likeness Score: -1.38

References

1. Metcalf B, Chuang C, Dufu K, Patel MP, Silva-Garcia A, Johnson C, Lu Q, Partridge JR, Patskovska L, Patskovsky Y, Almo SC, Jacobson MP, Hua L, Xu Q, Gwaltney SL, Yee C, Harris J, Morgan BP, James J, Xu D, Hutchaleelaha A, Paulvannan K, Oksenberg D, Li Z..  (2017)  Discovery of GBT440, an Orally Bioavailable R-State Stabilizer of Sickle Cell Hemoglobin.,  (3): [PMID:28337324] [10.1021/acsmedchemlett.6b00491]

Source